A rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes. [ Orphanet:732 https://orcid.org/0000-0001-5208-3432 ]
Synonyms: polymyositis PM
Term information
- NCIT:C26925 (MONDO:equivalentTo)
- MedDRA:10036102 (Orphanet:732/e)
- GARD:7425 (MONDO:GARD)
- Wikipedia:Polymyositis (EFO:0003063)
- NANDO:1200276 (https://orcid.org/0000-0003-0011-764X)
- MEDGEN:39086 (MONDO:equivalentTo)
- ICD10CM:M33.2 (Orphanet:732/e)
- MESH:D017285 (Orphanet:732/e)
- SCTID:31384009 (MONDO:equivalentTo)
- EFO:0003063 (MONDO:equivalentTo)
- Orphanet:732 (MONDO:equivalentTo)
- UMLS:C0085655 (MONDO:equivalentTo)
- icd11.foundation:1157134196 (Orphanet:732)
- ICD9:710.4 (MONDO:i2s)
- DOID:0080745 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, mondo_top_grouping_idiopathic_disease, ordo_disorder, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, mondo_top_grouping_musculoskeletal_system_disorder, matrix_included, matrix_llm__tag_existing_treatment_other, nord_rare, harrisons_view_inflammatory_disease, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, mondo_top_grouping_inflammatory_disease, harrisons_view_member, harrisons_view_musculoskeletal_system_disorder, orphanet_rare
http://identifiers.org/snomedct/31384009
http://purl.bioontology.org/ontology/ICD10CM/M33.2
http://www.orpha.net/ORDO/Orphanet_732
http://purl.obolibrary.org/obo/DOID_0080745
http://identifiers.org/mesh/D017285
http://www.ebi.ac.uk/efo/EFO_0003063
http://linkedlifedata.com/resource/umls/id/C0085655
http://purl.obolibrary.org/obo/NCIT_C26925
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1157134196
http://identifiers.org/medgen/39086